Medical Device Manufacturer · US , Mchenry , IL

Biologics Intl., Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1979

Total

Cleared

Denied

Biologics Intl., Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1979 to 1988. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Biologics Intl., Inc. Filter by specialty or product code using the sidebar.

Biologics Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biologics Intl., Inc.

9 devices

1-9 of 9

Cleared Aug 16, 1988

AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS

K882229 · IOQ

Physical Medicine · 88d

Biologics Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Biologics Intl., Inc.

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